Other mutations in this stock |
Total: 69 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
3110009E18Rik |
G |
C |
1: 120,096,840 (GRCm39) |
|
probably benign |
Het |
3110009E18Rik |
C |
T |
1: 120,096,850 (GRCm39) |
|
probably benign |
Het |
3110009E18Rik |
G |
T |
1: 120,096,849 (GRCm39) |
|
probably benign |
Het |
6820408C15Rik |
T |
A |
2: 152,286,013 (GRCm39) |
V342D |
probably damaging |
Het |
Arhgap33 |
C |
T |
7: 30,231,786 (GRCm39) |
G101R |
probably damaging |
Het |
Atf7ip |
C |
T |
6: 136,583,808 (GRCm39) |
R1280C |
probably damaging |
Het |
Cacnb4 |
T |
C |
2: 52,448,303 (GRCm39) |
H8R |
probably damaging |
Het |
Ccdc150 |
T |
A |
1: 54,404,027 (GRCm39) |
|
probably benign |
Het |
Cd74 |
A |
G |
18: 60,942,109 (GRCm39) |
N113D |
probably benign |
Het |
Cdc25b |
T |
C |
2: 131,035,525 (GRCm39) |
V341A |
possibly damaging |
Het |
Clptm1l |
T |
A |
13: 73,759,315 (GRCm39) |
I245N |
possibly damaging |
Het |
Clptm1l |
T |
C |
13: 73,760,547 (GRCm39) |
I310T |
probably damaging |
Het |
Creb5 |
A |
T |
6: 53,670,907 (GRCm39) |
|
probably null |
Het |
Crebbp |
T |
C |
16: 3,935,231 (GRCm39) |
Q460R |
probably benign |
Het |
Dnah17 |
A |
T |
11: 117,965,124 (GRCm39) |
I2306N |
probably benign |
Het |
Dync1h1 |
C |
A |
12: 110,624,560 (GRCm39) |
T3700N |
probably damaging |
Het |
Elovl1 |
A |
T |
4: 118,289,120 (GRCm39) |
H215L |
probably damaging |
Het |
Enkd1 |
A |
G |
8: 106,431,121 (GRCm39) |
I202T |
probably benign |
Het |
Epha7 |
C |
T |
4: 28,871,892 (GRCm39) |
A407V |
probably damaging |
Het |
Ercc3 |
G |
T |
18: 32,376,170 (GRCm39) |
G130W |
probably damaging |
Het |
Fbxl8 |
A |
G |
8: 105,994,827 (GRCm39) |
E113G |
probably damaging |
Het |
Frmpd1 |
T |
G |
4: 45,273,099 (GRCm39) |
N339K |
probably damaging |
Het |
Frrs1 |
G |
A |
3: 116,678,897 (GRCm39) |
D240N |
probably benign |
Het |
Gemin2 |
A |
G |
12: 59,063,954 (GRCm39) |
S105G |
probably benign |
Het |
Glra1 |
T |
A |
11: 55,418,224 (GRCm39) |
I257F |
probably damaging |
Het |
Gmcl1 |
G |
A |
6: 86,687,503 (GRCm39) |
P354S |
probably damaging |
Het |
Gpr15 |
G |
T |
16: 58,538,537 (GRCm39) |
A184E |
probably damaging |
Het |
Grm7 |
G |
A |
6: 111,335,824 (GRCm39) |
G745E |
probably damaging |
Het |
Hdac5 |
C |
A |
11: 102,096,082 (GRCm39) |
|
probably benign |
Het |
Ift22 |
G |
A |
5: 136,937,070 (GRCm39) |
|
probably benign |
Het |
Ighg3 |
T |
C |
12: 113,324,750 (GRCm39) |
E34G |
unknown |
Het |
Itga11 |
A |
T |
9: 62,674,930 (GRCm39) |
T821S |
probably benign |
Het |
Lmod2 |
T |
C |
6: 24,603,871 (GRCm39) |
V282A |
possibly damaging |
Het |
Maml2 |
A |
G |
9: 13,531,572 (GRCm39) |
K262R |
probably damaging |
Het |
Mme |
T |
A |
3: 63,250,910 (GRCm39) |
|
probably benign |
Het |
Mnat1 |
A |
G |
12: 73,170,652 (GRCm39) |
Y14C |
probably damaging |
Het |
Mtdh |
A |
T |
15: 34,083,281 (GRCm39) |
T34S |
possibly damaging |
Het |
Ncaph |
T |
C |
2: 126,963,177 (GRCm39) |
D352G |
possibly damaging |
Het |
Or2t43 |
A |
G |
11: 58,457,344 (GRCm39) |
Y276H |
probably damaging |
Het |
Or4f17-ps1 |
C |
A |
2: 111,358,569 (GRCm39) |
N321K |
probably benign |
Het |
Or5m9b |
T |
A |
2: 85,905,854 (GRCm39) |
Y257N |
probably damaging |
Het |
Or9g8 |
T |
C |
2: 85,607,459 (GRCm39) |
F177S |
probably damaging |
Het |
Pcdhb13 |
T |
A |
18: 37,577,837 (GRCm39) |
D738E |
possibly damaging |
Het |
Pla2g4f |
C |
T |
2: 120,130,980 (GRCm39) |
R825Q |
probably benign |
Het |
Pnliprp2 |
C |
T |
19: 58,763,577 (GRCm39) |
L409F |
possibly damaging |
Het |
Prlr |
G |
T |
15: 10,319,281 (GRCm39) |
C70F |
probably damaging |
Het |
Ptpn14 |
C |
T |
1: 189,583,469 (GRCm39) |
T772I |
probably benign |
Het |
Ryr2 |
T |
C |
13: 11,799,966 (GRCm39) |
Q927R |
probably damaging |
Het |
Scarf1 |
A |
G |
11: 75,416,460 (GRCm39) |
E634G |
probably benign |
Het |
Scart1 |
T |
C |
7: 139,808,435 (GRCm39) |
V782A |
probably damaging |
Het |
Skic3 |
T |
G |
13: 76,333,232 (GRCm39) |
|
probably null |
Het |
Slc39a14 |
A |
T |
14: 70,553,260 (GRCm39) |
S158R |
probably damaging |
Het |
Slc9c1 |
A |
T |
16: 45,365,194 (GRCm39) |
T176S |
probably benign |
Het |
Srsf10 |
T |
C |
4: 135,583,541 (GRCm39) |
S2P |
probably damaging |
Het |
Tcam1 |
T |
A |
11: 106,173,705 (GRCm39) |
C50S |
probably damaging |
Het |
Tcf7l2 |
A |
G |
19: 55,919,864 (GRCm39) |
|
probably null |
Het |
Tdrd3 |
T |
A |
14: 87,743,223 (GRCm39) |
H390Q |
probably benign |
Het |
Tlk2 |
T |
C |
11: 105,144,185 (GRCm39) |
|
probably null |
Het |
Tnc |
G |
C |
4: 63,894,793 (GRCm39) |
P1531R |
probably damaging |
Het |
Tnfrsf1b |
C |
A |
4: 144,973,327 (GRCm39) |
Q15H |
probably damaging |
Het |
Tnfrsf1b |
T |
G |
4: 144,973,328 (GRCm39) |
Q15P |
possibly damaging |
Het |
Tssk4 |
A |
T |
14: 55,889,266 (GRCm39) |
E264V |
probably damaging |
Het |
Ugt3a1 |
G |
A |
15: 9,365,274 (GRCm39) |
V296I |
probably benign |
Het |
Usp5 |
C |
G |
6: 124,799,593 (GRCm39) |
K318N |
possibly damaging |
Het |
Vmn2r8 |
T |
G |
5: 108,947,129 (GRCm39) |
E541A |
probably benign |
Het |
Ybx1 |
A |
T |
4: 119,136,135 (GRCm39) |
|
probably benign |
Het |
Zfp39 |
T |
A |
11: 58,782,057 (GRCm39) |
Y235F |
possibly damaging |
Het |
Zfp422 |
T |
A |
6: 116,603,904 (GRCm39) |
K32* |
probably null |
Het |
Zpbp2 |
T |
A |
11: 98,442,150 (GRCm39) |
|
probably null |
Het |
|
Other mutations in H2-T10 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01296:H2-T10
|
APN |
17 |
36,431,602 (GRCm39) |
missense |
probably benign |
0.08 |
IGL01946:H2-T10
|
APN |
17 |
36,431,608 (GRCm39) |
missense |
possibly damaging |
0.45 |
IGL03367:H2-T10
|
APN |
17 |
36,431,285 (GRCm39) |
missense |
possibly damaging |
0.81 |
IGL03381:H2-T10
|
APN |
17 |
36,430,249 (GRCm39) |
nonsense |
probably null |
|
IGL03381:H2-T10
|
APN |
17 |
36,430,246 (GRCm39) |
missense |
probably benign |
|
FR4304:H2-T10
|
UTSW |
17 |
36,431,173 (GRCm39) |
frame shift |
probably null |
|
R0305:H2-T10
|
UTSW |
17 |
36,430,260 (GRCm39) |
missense |
probably damaging |
1.00 |
R1446:H2-T10
|
UTSW |
17 |
36,430,266 (GRCm39) |
missense |
possibly damaging |
0.87 |
R1483:H2-T10
|
UTSW |
17 |
36,432,038 (GRCm39) |
missense |
probably benign |
0.44 |
R2038:H2-T10
|
UTSW |
17 |
36,430,317 (GRCm39) |
missense |
probably benign |
0.00 |
R2402:H2-T10
|
UTSW |
17 |
36,428,631 (GRCm39) |
splice site |
probably null |
|
R4755:H2-T10
|
UTSW |
17 |
36,429,837 (GRCm39) |
nonsense |
probably null |
|
R5162:H2-T10
|
UTSW |
17 |
36,429,843 (GRCm39) |
splice site |
probably null |
|
R5568:H2-T10
|
UTSW |
17 |
36,430,079 (GRCm39) |
critical splice donor site |
probably null |
|
R6226:H2-T10
|
UTSW |
17 |
36,431,975 (GRCm39) |
missense |
probably damaging |
0.99 |
R6850:H2-T10
|
UTSW |
17 |
36,430,152 (GRCm39) |
missense |
probably damaging |
1.00 |
R7249:H2-T10
|
UTSW |
17 |
36,430,269 (GRCm39) |
missense |
probably damaging |
0.99 |
R7324:H2-T10
|
UTSW |
17 |
36,430,189 (GRCm39) |
missense |
probably damaging |
1.00 |
R7466:H2-T10
|
UTSW |
17 |
36,431,741 (GRCm39) |
missense |
probably benign |
0.10 |
R7679:H2-T10
|
UTSW |
17 |
36,430,216 (GRCm39) |
missense |
not run |
|
R7767:H2-T10
|
UTSW |
17 |
36,428,622 (GRCm39) |
missense |
probably benign |
0.02 |
R7901:H2-T10
|
UTSW |
17 |
36,431,143 (GRCm39) |
missense |
probably benign |
|
R8278:H2-T10
|
UTSW |
17 |
36,429,832 (GRCm39) |
missense |
probably benign |
0.00 |
R8315:H2-T10
|
UTSW |
17 |
36,429,905 (GRCm39) |
missense |
probably benign |
0.41 |
R9646:H2-T10
|
UTSW |
17 |
36,431,157 (GRCm39) |
missense |
probably damaging |
0.96 |
RF032:H2-T10
|
UTSW |
17 |
36,431,186 (GRCm39) |
frame shift |
probably null |
|
RF046:H2-T10
|
UTSW |
17 |
36,431,186 (GRCm39) |
frame shift |
probably null |
|
|